Site Activation Manager (evergreen)
IQVIA(1 year ago)
About this role
This role leads regulatory and site activation efforts for clinical studies and multi-protocol programs, supporting study initiation and maintenance across regions. It provides regulatory and scientific input for pre-award and business development activities and contributes regulatory intelligence to support program execution. The position partners with study management teams and clients to ensure compliant delivery of study authorizations and approvals.
Required Skills
- Site Activation
- Regulatory Strategy
- Project Management
- Budget Management
- Technical Writing
- GCP
- ICH
- Leadership
- Stakeholder Management
- Quality Management
+4 more
Qualifications
- Bachelor's Degree Life Sciences
About IQVIA
iqvia.comIQVIA is a leading global provider of data, technology, and advanced analytics focused on transforming healthcare and life sciences. The company empowers organizations to accelerate innovation, enhance patient outcomes, and expedite the market introduction of new treatments through comprehensive healthcare analytics and real-world evidence. With a commitment to Human Data Science, IQVIA combines its extensive expertise with innovative technology to improve health outcomes worldwide.
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